With the aim of providing better clinical characterisation of patients with α1-antitrypsin deficiency (AATD), we analysed the data of adult patients with severe AATD enrolled in the Spanish and Italian national registries. We assessed 745 subjects, 416 of whom were enrolled in the Spanish registry and 329 in the Italian registry. 57.2\% were male and 64.9\% were smokers or former smokers with a mean±sd age of 49.9±13.8 years. Most (81.2\%) were index cases, mainly having the PI*ZZ genotype (73.4\%), and the mean±sd diagnostic delay was 9.0±12.1 years. Patients with chronic bronchitis were younger, had better preserved lung function and lower tobacco consumption. Overlap patients (chronic obstructive pulmonary disease with asthma) were mainl...
α1-antitrypsin deficiency (AATD) is the most common hereditary disorder in adults. It is associated ...
AATD is one of the most common inherited disorders in the World. However, it is generally accepted t...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
With the aim of providing better clinical characterisation of patients with α1-antitrypsin deficienc...
The Spanish registry of α1-antitrypsin deficiency (AATD) integrated in the European Alpha-1 Research...
Targeted detection programmes are recommended to identify subjects affected by severe alpha1-antitry...
SummaryTargeted detection programmes are recommended to identify subjects affected by severe alpha1-...
Spanish registry; Clinical characteristicsRegistre espanyol; Característiques clíniquesRegistro espa...
Over the past 10–15 years, the diagnosis of α1-antitrypsin deficiency (AATD) has markedly improved a...
Abstractα1-antitrypsin (AAT) deficiency is an inherited condition characterized by low serum levels ...
Alpha1-antitrypsin deficiency (AATD) is a genetic condition associated with an increased risk of de...
AbstractSevere alpha-1-antitrypsin (AAT) deficiency, phenotype Pi ZZ, is a rare condition with an es...
α1-antitrypsin deficiency (AATD) is a hereditary disorder associated with a risk of developing liver...
Alpha-1 Antitrypsin Deficiency (AATD), characterised by reduced levels or functionality of Alpha-1 A...
Critical to the effective diagnosis and management of disease is information on its prevalence in a ...
α1-antitrypsin deficiency (AATD) is the most common hereditary disorder in adults. It is associated ...
AATD is one of the most common inherited disorders in the World. However, it is generally accepted t...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...
With the aim of providing better clinical characterisation of patients with α1-antitrypsin deficienc...
The Spanish registry of α1-antitrypsin deficiency (AATD) integrated in the European Alpha-1 Research...
Targeted detection programmes are recommended to identify subjects affected by severe alpha1-antitry...
SummaryTargeted detection programmes are recommended to identify subjects affected by severe alpha1-...
Spanish registry; Clinical characteristicsRegistre espanyol; Característiques clíniquesRegistro espa...
Over the past 10–15 years, the diagnosis of α1-antitrypsin deficiency (AATD) has markedly improved a...
Abstractα1-antitrypsin (AAT) deficiency is an inherited condition characterized by low serum levels ...
Alpha1-antitrypsin deficiency (AATD) is a genetic condition associated with an increased risk of de...
AbstractSevere alpha-1-antitrypsin (AAT) deficiency, phenotype Pi ZZ, is a rare condition with an es...
α1-antitrypsin deficiency (AATD) is a hereditary disorder associated with a risk of developing liver...
Alpha-1 Antitrypsin Deficiency (AATD), characterised by reduced levels or functionality of Alpha-1 A...
Critical to the effective diagnosis and management of disease is information on its prevalence in a ...
α1-antitrypsin deficiency (AATD) is the most common hereditary disorder in adults. It is associated ...
AATD is one of the most common inherited disorders in the World. However, it is generally accepted t...
Despite recent improvements, α1-antitrypsin deficiency (AATD) remains a rarely diagnosed and treated...